S. Tinschert: search on Z-Library

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1

[IEEE 2011 IEEE International Ultrasonics Symposium (IUS) - Orlando, FL, USA (2011.10.18-2011.10.21)] 2011 IEEE International Ultrasonics Symposium - High frequency (75MHz) ultrasound based tooth digitization using sparse spatial compounding

Heger, Stefan, Vollborn, Thorsten, Tinschert, Joachim, Chuembou, Fabrice, Wolfart, Stefan, Radermacher, Klaus

Year:

2011

Language:

english

File:

PDF, 357 KB

english, 2011

2

Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor

Plaschke, Jens, Linnebacher, Michael, Kloor, Matthias, Gebert, Johannes, Cremer, Friedrich W, Tinschert, Sigrid, Aust, Daniela E, von Knebel Doeberitz, Magnus, Schackert, Hans K

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 191 KB

english, 2006

3

Two independent mutations in a family with neurofibromatosis type 1 (NF1)

Klose, Anja, Peters, Hartmut, Hoffmeyer, Sven, Buske, Annegret, L�der, Andrea, He�, Detlef, Lehmann, R�diger, N�rnberg, Peter, Tinschert, Sigrid

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 565 KB

english, 1999

4

Three novel mutations of the NF1 gene detected by temperature gradient gel electrophoresis of exons 5 and 8

Denise Horn, Peter N. Robinson, Annett Böddrich, Annegret Buske, Sigrid Tinschert, Dr. Peter Nürnberg

Journal:

ELECTROPHORESIS

Year:

1996

Language:

english

File:

PDF, 517 KB

english, 1996

5

Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene

Tinschert, Sigrid, Naumann, Ilka, Stegmann, Elisabeth, Buske, Annegret, Kaufmann, Dieter, Thiel, Gundula, Jenne, Dieter E

Journal:

European Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 163 KB

english, 2000

6

Emittance estimation by an ion optical element with variable focusing strength and a viewing target

Mäder, J., Roßbach, J., Maimone, F., Spädtke, P., Tinschert, K., Lang, R., Sun, L., Cao, Y., Zhao, H.

Journal:

Review of Scientific Instruments

Year:

2010

Language:

english

File:

PDF, 639 KB

english, 2010

7

[IEEE 2013 15th European Conference on Power Electronics and Applications (EPE) - Lille, France (2013.09.2-2013.09.6)] 2013 15th European Conference on Power Electronics and Applications (EPE) - Evaluation of the submodel technique for FEM simulations of power electronic housings under power cycling conditions

Tinschert, Lukas, Hofmann, Kay, Poller, Tilo, Lutz, Josef

Year:

2013

File:

PDF, 446 KB

2013

8

Influence of frequency tuning and double-frequency heating on ions extracted from an electron cyclotron resonance ion source

F. Maimone, L. Celona, R. Lang, J. Mäder, J. Roßbach, P. Spädtke, K. Tinschert

Year:

2011

Language:

english

File:

PDF, 3.16 MB

english, 2011

9

Low-energy high-intensity extraction system for CHORDIS

K. Tinschert, W. Zhao

Year:

1992

Language:

english

File:

PDF, 665 KB

english, 1992

10

Electron cyclotron resonance ion sources in use for heavy ion cancer therapy

Tinschert, K., Iannucci, R., Lang, R.

Journal:

Review of Scientific Instruments

Year:

2008

Language:

english

File:

PDF, 452 KB

english, 2008

11

Ion source development at GSI

Spädtke, P., Bossler, J., Emig, H., Leible, K. D., Mühle, C., Reich, H., Schulte, H., Tinschert, K.

Journal:

Review of Scientific Instruments

Year:

1998

Language:

english

File:

PDF, 345 KB

english, 1998

12

Possible failure modes in Press-Pack IGBTs

Tinschert, Lukas, Årdal, Atle Rygg, Poller, Tilo, Bohlländer, Marco, Hernes, Magnar, Lutz, Josef

Journal:

Microelectronics Reliability

Year:

2015

Language:

english

File:

PDF, 2.83 MB

english, 2015

13

Electron cyclotron resonance ion source experience at the Heidelberg Ion Beam Therapy Center

Winkelmann, T., Cee, R., Haberer, T., Naas, B., Peters, A., Scheloske, S., Spädtke, P., Tinschert, K.

Journal:

Review of Scientific Instruments

Year:

2008

Language:

english

File:

PDF, 483 KB

english, 2008

14

Tetraphocomelia and bilateral cleft lip in a historical case of Roberts syndrome [Virchow, 1898]

Urban, Maik, Rogalla, Patrik, Tinschert, Sigrid, Krietsch, Peter

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 459 KB

english, 1997

15

Craniometaphyseal dysplasia in six generations of a German kindred

Tinschert, Sigrid, Braun, Hans-Steffen

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 721 KB

english, 1998

16

Bilaterally cleft lip, limb defects, and haematological manifestations: Roberts syndrome versus TAR syndrome

Urban, Maik, Opitz, Charlotte, Bommer, Christiane, Enders, Herbert, Tinschert, Sigrid, Witkowski, Regine

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 342 KB

english, 1998

17

McCune-Albright syndrome: Clinical and molecular evidence of mosaicism in an unusual giant patient

Tinschert, Sigrid, Gerl, Helga, Gewies, Andreas, Jung, Hans-Peter, N�rnberg, Peter

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 546 KB

english, 1999

18

RecurrentNF1 gene mutation in a patient with oligosymptomatic neurofibromatosis type 1 (NF1)

Buske, Annegret, Gewies, Andreas, Lehmann, R�diger, R�ther, Klaus, Algermissen, Bernd, N�rnberg, Peter, Tinschert, Sigrid

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 52 KB

english, 1999

19

Fetal trisomy 10 mosaicism: ultrasound, cytogenetic and morphologic findings in early pregnancy

H. Knoblauch, D. Sommer, C. Zimmer, C. Tennstedt, K. Heling, R. Bollmann, C. Bommer, S. Tinschert, H. Körner

Journal:

Prenatal Diagnosis

Year:

1999

Language:

english

File:

PDF, 156 KB

english, 1999

20

Recurrent 2-bp deletion in exon 10c of the NF1 gene in two cases of von Recklinghausen neurofibromatosis

Peter N. Robinson, Annegret Buske, Regina Neumann, Sigrid Tinschert, Peter Nürnberg

Journal:

Year:

1996

Language:

english

File:

PDF, 297 KB

english, 1996

21

New evidence for a mutation hotspot in exon 37 of the NF1 gene

Annett Böddrich, Peter N. Robinson, Markus Schülke, Annegret Buske, Sigrid Tinschert, Peter Nürnberg

Journal:

Year:

1997

Language:

english

File:

PDF, 132 KB

english, 1997

22

Mutation screening of neurofibromatosis type 1 (NF1) exons 28 and 29 with single strand conformation polymorphism (SSCP): Five novel mutations, one recurrent transition and two polymorphisms in a panel of 118 unrelated NF1 patients

Hartmut Peters, Andrea Lüder, Anja Harder, Markus Schuelke, Sigrid Tinschert

Journal:

Year:

1999

Language:

english

File:

PDF, 17 KB

english, 1999

23

A novel 5-bp deletion in exon 30 of the neurofibromatosis type 1 (NF1) gene

Anja Harder, Carmen Macsuga, Sigrid Tinschert, Peter Nürnberg, Hartmut Peters

Journal:

Year:

1999

Language:

english

File:

PDF, 9 KB

english, 1999

24

Analysis of the NF1 gene by temperature gradient gel electrophoresis reveals a high incidence of mutations in exon 4b

Mohammed R. Toliat, Fikret Erdogan, Andreas Gewies, Raimund Fahsold, Annegret Buske, Sigrid Tinschert, Peter Nürnberg

Journal:

ELECTROPHORESIS

Year:

2000

Language:

english

File:

PDF, 116 KB

english, 2000

25

Metaphyseal dysplasia: A new autosomal dominant type in a large German kindred

Hans-Steffen Braun, Peter Nürnberg, Sigrid Tinschert

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 202 KB

english, 2001

26

Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families

Constance Schrander-Stumpel, Chris Höweler, Marilyn Jones, Annemarie Sommer, Cathy Stevens, Sigrid Tinschert, Jeanette Israel, Jean Pierre Fryns

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 1.10 MB

english, 1995

27

Maik urban 1966–2000

Alexa Nieschlag, Sigrid Tinschert

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 89 KB

english, 2001

28

Antenatal onset of cortical hyperostosis (Caffey disease): Case report and review

Susann Schweiger, Rabih Chaoui, Cornelia Tennstedt, Katarina Lehmann, Stefan Mundlos, Sigrid Tinschert

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 220 KB

english, 2003

29

Two brothers with findings resembling congenital intrauterine infection-like syndrome (pseudo-TORCH syndrome)

Hans Knoblauch, Cornelia Tennstedt, Wolfgang Brueck, Hannes Hammer, Tom Vulliamy, Inderjeet Dokal, Rüdiger Lehmann, Folker Hanefeld, Sigrid Tinschert

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 140 KB

english, 2003

30

Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation

Ulrike A. Nuber, Sigrid Tinschert, Stefan Mundlos, Ingrid Hauber

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 410 KB

english, 2004

31

Response to Kosaki et al. “Molecular pathology of Shprintzen–Goldberg syndrome”

Peter N. Robinson, Luitgard M. Neumann, Sigrid Tinschert

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 62 KB

english, 2006

32

Czech dysplasia: Report of a large family and further delineation of the phenotype

Andreas Tzschach, Sigrid Tinschert, Elke Kaminsky, Eugen Lusga, Stefan Mundlos, Luitgard M. Graul-Neumann

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 217 KB

english, 2008

33

Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss

Uwe Kornak, Francesco Brancati, Martine Le Merrer, Klaske Lichtenbelt, Wolfgang Höhne, Sigrid Tinschert, Francesco Giuseppe Garaci, Bruno Dallapiccola, Peter Nürnberg

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 221 KB

english, 2010

34

Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia

Volker Endris, Karl Hackmann, Teresa M. Neuhann, Ute Grasshoff, Michael Bonin, Ulrich Haug, Gabriele Hahn, Jens C. Schallner, Evelin Schröck, Sigrid Tinschert, Gudrun Rappold, Ute Moog

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 102 KB

english, 2010

35

A new autosomal dominant syndrome of distinctive face showing ptosis and prominent eyes associated with cleft palate, ear anomalies, and learning disability

N. Tyshchenko, T.M. Neuhann, E. Gerlach, G. Hahn, K. Heisch, A. Rump, E. Schrock, S. Tinschert, K. Hackmann

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 299 KB

english, 2011

36

Detection of novel NF1 mutations and rapid mutation prescreening with Pyrosequencing

Anja Brinckmann, Claudia Mischung, Ingelore Bässmann, Jirko Kühnisch, Markus Schuelke, Sigrid Tinschert, Peter Nürnberg

Journal:

ELECTROPHORESIS

Year:

2007

Language:

english

File:

PDF, 315 KB

english, 2007

37

Complete physical map and gene content of the human NF1 tumor suppressor region in human and mouse

Dieter E. Jenne, Sigrid Tinschert, Michael O. Dorschner, Horst Hameister, Karen Stephens, Hildegard Kehrer-Sawatzki

Journal:

Genes, Chromosomes and Cancer

Year:

2003

Language:

english

File:

PDF, 1005 KB

english, 2003

38

Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patients

K. Wimmer, S. Yao, K. Claes, H. Kehrer-Sawatzki, S. Tinschert, T. De Raedt, E. Legius, T. Callens, H. Beiglböck, O. Maertens, L. Messiaen

Journal:

Genes, Chromosomes and Cancer

Year:

2006

Language:

english

File:

PDF, 1.10 MB

english, 2006

39

Screening 500 unselected neurofibromatosis 1 patients for deletions of the NF1 gene

Lan Kluwe, Reiner Siebert, Stefan Gesk, Reinhard E. Friedrich, Sigrid Tinschert, Hildegard Kehrer-Sawatzki, Victor-F. Mautner

Journal:

Year:

2004

Language:

english

File:

PDF, 253 KB

english, 2004

40

A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2

Kathrin Bengesser, David N. Cooper, Katharina Steinmann, Lan Kluwe, Nadia A. Chuzhanova, Katharina Wimmer, Marcos Tatagiba, Sigrid Tinschert, Victor-Felix Mautner, Hildegard Kehrer-Sawatzki

Journal:

Year:

2010

Language:

english

File:

PDF, 290 KB

english, 2010

41

Intronic mutations in the L1CAM gene may cause X-linked hydrocephalus by aberrant splicing

Christian A. Hübner, Barbara Utermann, Sigrid Tinschert, Gabriele Krüger, Bernadette Ressler, Cordula Steglich, Albert Schinzel, Andreas Gal

Journal:

Year:

2004

Language:

english

File:

PDF, 36 KB

english, 2004

42

Lifetime of alumina- and zirconia ceramics used for crown and bridge restorations

Joachim Tinschert, Gerd Natt, Nina Mohrbotter, Hubertus Spiekermann, Karen A. Schulze

Journal:

Journal of Biomedical Materials Research Part B: Applied Biomaterials

Year:

2007

Language:

english

File:

PDF, 165 KB

english, 2007

43

Separation of androsterone from epiandrosterone, and dehydroepiandrosterone from its 3-hydroxy epimer by thin-layer cromatography

W. Tinschert, L. Träger

Journal:

Journal of Chromatography A

Year:

1978

Language:

english

File:

PDF, 457 KB

english, 1978

44

MIA is a potential biomarker for tumour load in neurofibromatosis type 1

Mateusz Kolanczyk, Victor Mautner, Nadine Kossler, Rosa Nguyen, Jirko Kühnisch, Tomasz Zemojtel, Aleksander Jamsheer, Eike Wegener, Boris Thurisch, Sigrid Tinschert, Nikola Holtkamp, Su-Jin Park, Patr

Journal:

Year:

2011

Language:

english

File:

PDF, 1.09 MB

english, 2011

45

Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 gene

Peter N. Robinson, Annett Böddrich, Hartmut Peters, Sigrid Tinschert, Annegret Buske, Dieter Kaufmann, Peter Nürnberg

Journal:

Year:

1995

Language:

english

File:

PDF, 691 KB

english, 1995

46

Maternal serum alpha-fetoprotein screening for neural tube defects and other disorders using an ultramicro-ELISA

Hannelore Körner, Lidia Rodriguez, J. L. Fernandez Yero, Margarete Schulze, Anton Horn, L. Heredero, Regine Witkowski, Sigrid Tinschert, J. Oliva, Dietlind Sommer, R. Solis, Ch. Zwahr, P. Prenzlau, G.

Journal:

Year:

1986

Language:

english

File:

PDF, 324 KB

english, 1986

47

Resonances in the electron-impact single and multiple ionization of ions

G. Hofmann, A. Müller, B. Weißbecker, M. Stenke, K. Tinschert, E. Salzborn

Journal:

Zeitschrift für Physik D Atoms, Molecules and Clusters

Year:

1991

Language:

english

File:

PDF, 348 KB

english, 1991

48

Doubly autoionizing capture resonances ine+ Mg+collisions

A. Müller, G. Hofmann, K. Tinschert, B. Weißbecker, E. Salzborn

Journal:

Zeitschrift für Physik D Atoms, Molecules and Clusters

Year:

1990

Language:

english

File:

PDF, 606 KB

english, 1990

49

Indirect processes in the electron-impact ionization of Li-like ions

G. Hofmann, A. Müller, K. Tinschert, E. Salzborn

Journal:

Zeitschrift für Physik D Atoms, Molecules and Clusters

Year:

1990

Language:

english

File:

PDF, 1.91 MB

english, 1990

50

The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients

C. Schrander-Stumpel, P. Meinecke, G. Wilson, G. Gilleseen-Kaesbach, S. Tinschert, R. König, N. Philip, R. Rizzo, J. Schrander, L. Pfeiffer, A. Maat-Kievit, I. van der Burgt, T. van Essen, E. Latta, U

Journal:

European Journal of Pediatrics

Year:

1994

Language:

english

File:

PDF, 2.49 MB

english, 1994

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